WASF1-SLC41A3 Fusion FISH Probe
The WASF1-SLC41A3 Fusion FISH Probe is used to confirm a fusion of the WASF1 and SLC41A3 genes. The fusion of the WASF1 and SLC41A3 genes has been associated with Sarcoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| WASF1-SLC41A3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-RERE | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-REOR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-REGO | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-REGR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-REAQ | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-ORRE | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-OROR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-ORGO | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-ORAQ | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GORE | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GOOR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GOGO | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GOGR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GOAQ | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GRRE | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GROR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GRGO | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GRGR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-GRAQ | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-AQRE | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-AQOR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-AQGO | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-AQGR | 20 (40 μL) | 200 μL |
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| WASF1-SLC41A3-20-AQAQ | 20 (40 μL) | 200 μL |
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WASF1 Gene Summary
The protein encoded by this gene, a member of the Wiskott-Aldrich syndrome protein (WASP)-family, plays a critical role downstream of Rac, a Rho-family small GTPase, in regulating the actin cytoskeleton required for membrane ruffling. It has been shown to associate with an actin nucleation core Arp2/3 complex while enhancing actin polymerization in vitro. Wiskott-Aldrich syndrome is a disease of the immune system, likely due to defects in regulation of actin cytoskeleton. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: WAS Protein Family Member 1
Chromosome: CHR6: 110421021 -110501207
Locus: 6q21
SLC41A3 Gene Summary
The Solute Carrier Family 41 Member 3 (SLC41A3) gene is located on chr3 :125725199-125820391 at 3q21.2-q21.3.
Gene Name: Solute Carrier Family 41 Member 3
Chromosome: CHR3: 125725199 -125820391
Locus: 3q21.2-q21.3
Gene Diseases
The WASF1 SLC41A3 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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